ES2139754T3 - 3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS. - Google Patents

3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS.

Info

Publication number
ES2139754T3
ES2139754T3 ES94927778T ES94927778T ES2139754T3 ES 2139754 T3 ES2139754 T3 ES 2139754T3 ES 94927778 T ES94927778 T ES 94927778T ES 94927778 T ES94927778 T ES 94927778T ES 2139754 T3 ES2139754 T3 ES 2139754T3
Authority
ES
Spain
Prior art keywords
pct
date
isoxazolines
sec
aryl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES94927778T
Other languages
Spanish (es)
Inventor
Edward F Kleinman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Inc
Original Assignee
Pfizer Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Inc filed Critical Pfizer Inc
Application granted granted Critical
Publication of ES2139754T3 publication Critical patent/ES2139754T3/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/04Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6527Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07F9/653Five-membered rings

Abstract

PCT No. PCT/IB94/00313 Sec. 371 Date May 15, 1996 Sec. 102(e) Date May 15, 1996 PCT Filed Oct. 12, 1994 PCT Pub. No. WO95/14680 PCT Pub. Date Jun. 1, 1995This invention relates to 3-aryl-2-isoxazoline compounds which are selective inhibitors of phosphodiesterase type IV (PDEIV). The 3-aryl-2-isoxazolines are useful in the treatment of AIDS, asthma, arthritis, bronchitis, chronic obstructive pulmonary disease, psoriasis, allergic rhinitis, dermatitis, shock, atopic dermatitis, rheumatoid arthritis and osteoarthritis. This invention also relates to pharmaceutical compositions useful therefor.
ES94927778T 1993-11-26 1994-10-12 3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS. Expired - Lifetime ES2139754T3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US15724193A 1993-11-26 1993-11-26

Publications (1)

Publication Number Publication Date
ES2139754T3 true ES2139754T3 (en) 2000-02-16

Family

ID=22562909

Family Applications (1)

Application Number Title Priority Date Filing Date
ES94927778T Expired - Lifetime ES2139754T3 (en) 1993-11-26 1994-10-12 3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS.

Country Status (12)

Country Link
US (1) US5686434A (en)
EP (1) EP0730587B1 (en)
JP (1) JP2818820B2 (en)
AT (1) ATE187447T1 (en)
CA (1) CA2177375A1 (en)
DE (1) DE69422061T2 (en)
DK (1) DK0730587T3 (en)
ES (1) ES2139754T3 (en)
FI (1) FI945556A (en)
GR (1) GR3032506T3 (en)
PT (1) PT730587E (en)
WO (1) WO1995014680A1 (en)

Families Citing this family (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK0920421T3 (en) * 1996-08-21 2003-03-10 Upjohn Co Isoxazoline derivatives useful as antimicrobial agents
PT937075E (en) * 1996-11-11 2004-05-31 Altana Pharma Ag NEW IMIDAZO- AND OXAZOLO-PYRIDINES AS PHOSPHODIESTERESE INHIBITORS
US6124469A (en) * 1997-01-17 2000-09-26 Basf Aktiengesellschaft Process for preparing sulphurous 2-chloro-3-(4,5-dihydroisoxazol-3-yl)-benzoic acids
US6022977A (en) 1997-03-26 2000-02-08 Dupont Pharmaceuticals Company Dynamic resolution of isoxazoline thioesters to isoxazoline carboxylic acids
WO1999041244A1 (en) * 1998-02-13 1999-08-19 Pharmacia & Upjohn Company Substituted aminophenyl isoxazoline derivatives useful as antimicrobials
DE19852095A1 (en) 1998-11-12 2000-05-18 Basf Ag Process for the preparation of 2-alkyl-3- (4,5-dihydroisoxazol-3-yl) acylbenzenes
CA2652071C (en) * 1998-05-11 2012-01-17 Basf Aktiengesellschaft Method for producing isoxazoline-3-yl-acyl benzene
JP2002527438A (en) * 1998-10-09 2002-08-27 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 4,5-Dihydro-isoxazole derivatives and their pharmaceutical use
ES2260043T3 (en) 1999-08-21 2006-11-01 Altana Pharma Ag SYNERGIC COMBINATION OF ROFLUMILAST AND SALMETEROL.
KR100399361B1 (en) 1999-11-04 2003-09-26 주식회사 엘지생명과학 Therapeutic composition comprising caspase inhibitor
ATE273705T1 (en) * 1999-09-17 2004-09-15 Lg Chem Investment Ltd CASPASE INHIBITORS
DE19953024A1 (en) 1999-11-04 2001-05-10 Merck Patent Gmbh Isoxazole derivatives as phosphodiesterase VII inhibitors
US20030129186A1 (en) 2001-07-25 2003-07-10 Biomarin Pharmaceutical Inc. Compositions and methods for modulating blood-brain barrier transport
US7772188B2 (en) 2003-01-28 2010-08-10 Ironwood Pharmaceuticals, Inc. Methods and compositions for the treatment of gastrointestinal disorders
CA2517487A1 (en) 2003-04-01 2004-10-14 Applied Research Systems Ars Holding N.V. Inhibitors of phosphodiesterases in infertility
KR100594544B1 (en) * 2003-08-27 2006-06-30 주식회사 엘지생명과학 Caspase inhibitors containing isoxazoline ring
JP2007504123A (en) * 2003-08-29 2007-03-01 ランバクシー ラボラトリーズ リミテッド Inhibitors of type IV phosphodiesterase
WO2005051931A2 (en) * 2003-11-26 2005-06-09 Ranbaxy Laboratories Limited Phosphodiesterase inhibitors
CN101098697B (en) * 2004-03-26 2010-11-10 塞托凯恩药物科学公司 Compounds, compositions, processes of making, and methods of use related to inhibiting macrophage migration inhibitory factor
KR101195351B1 (en) * 2004-06-17 2012-10-29 인피니티 디스커버리, 인코포레이티드 Compounds and methods for inhibiting the interaction of bcl proteins with binding partners
ES2370788T3 (en) * 2005-02-07 2011-12-22 Aerocrine Ab CHECK BREATHED BREATH FLOW DURING ANALYSIS.
CN103156845B (en) * 2005-03-15 2015-11-18 翁科诺克斯有限公司 There is the compound of immunoregulatory activity
CN101287411B (en) 2005-04-28 2013-03-06 普罗秋斯生物医学公司 Pharma-informatics system
EP2258358A3 (en) 2005-08-26 2011-09-07 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
EP1928437A2 (en) 2005-08-26 2008-06-11 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
WO2007029077A1 (en) * 2005-09-05 2007-03-15 Ranbaxy Laboratories Limited Substituted indazoles as inhibitors of phosphodiesterase type-iv
RU2008119322A (en) * 2005-10-19 2009-11-27 Рэнбакси Лабораториз Лимитед (In) COMPOSITIONS OF PHOSPHODIESTHESIS INHIBITORS TYPE IV
EP2377530A3 (en) 2005-10-21 2012-06-20 Braincells, Inc. Modulation of neurogenesis by PDE inhibition
AU2006308889A1 (en) 2005-10-31 2007-05-10 Braincells, Inc. GABA receptor mediated modulation of neurogenesis
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
US7678808B2 (en) 2006-05-09 2010-03-16 Braincells, Inc. 5 HT receptor mediated neurogenesis
WO2007134136A2 (en) 2006-05-09 2007-11-22 Braincells, Inc. Neurogenesis by modulating angiotensin
US7998971B2 (en) * 2006-09-08 2011-08-16 Braincells Inc. Combinations containing a 4-acylaminopyridine derivative
MX2009002893A (en) 2006-09-18 2009-07-10 Raptor Pharmaceutical Inc Treatment of liver disorders by administration of receptor-associated protein (rap)-conjugates.
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
US20100029728A1 (en) * 2006-09-22 2010-02-04 Ranbaxy Laboratories Limited Phosphodiesterase inhibitors
KR20090069309A (en) * 2006-09-22 2009-06-30 랜박시 래보러터리스 리미티드 Inhibitors of phosphodiesterase type-iv
MX2009013293A (en) 2007-06-04 2010-02-15 Synergy Pharmaceuticals Inc Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders.
US8969514B2 (en) 2007-06-04 2015-03-03 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
ES2627848T3 (en) 2008-06-04 2017-07-31 Synergy Pharmaceuticals Inc. Guanylate cyclase agonists useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
JP2011528375A (en) 2008-07-16 2011-11-17 シナジー ファーマシューティカルズ インコーポレイテッド Guanylate cyclase agonists useful for the treatment of gastrointestinal disorders, inflammation, cancer, and other disorders
CA2752373C (en) 2009-02-20 2017-10-10 To-Bbb Holding B.V. Glutathione-based drug delivery system
WO2010099217A1 (en) 2009-02-25 2010-09-02 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
KR20180114970A (en) 2009-05-06 2018-10-19 라보라토리 스킨 케어, 인크. Dermal delivery compositions comprising active agent-calcium phosphate particle complexes and methods of using the same
CN101781294B (en) * 2010-03-10 2012-02-01 天津药物研究院 Imidazole derivative, and preparation method and application thereof
US9616097B2 (en) 2010-09-15 2017-04-11 Synergy Pharmaceuticals, Inc. Formulations of guanylate cyclase C agonists and methods of use
US20120077778A1 (en) 2010-09-29 2012-03-29 Andrea Bourdelais Ladder-Frame Polyether Conjugates
CN108676076A (en) 2011-03-01 2018-10-19 辛纳吉制药公司 The method for preparing guanosine cyclic mono-phosphate agonist
EP2691379B1 (en) 2011-03-31 2016-11-02 Bayer Intellectual Property GmbH Herbicidally and fungicidally active 3-phenylisoxazoline-5-carboxamides and 3-phenylisoxazoline-5-thioamides
EP2804603A1 (en) 2012-01-10 2014-11-26 President and Fellows of Harvard College Beta-cell replication promoting compounds and methods of their use
JP6472382B2 (en) 2012-09-25 2019-02-20 バイエル・クロップサイエンス・アクチェンゲゼルシャフト 3-Phenylisoxazoline derivative having herbicidal effect
KR102040740B1 (en) * 2012-09-25 2019-11-05 바이엘 크롭사이언스 악티엔게젤샤프트 Herbicidal and fungicidal 5-oxy-substituted 3-phenylisoxazoline-5-carboxamides and 5-oxy-substituted 3-phenylisoxazoline-5-thioamides
US9545446B2 (en) 2013-02-25 2017-01-17 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase and their uses
AU2014235209B2 (en) 2013-03-15 2018-06-14 Bausch Health Ireland Limited Guanylate cyclase receptor agonists combined with other drugs
JP2016514671A (en) 2013-03-15 2016-05-23 シナジー ファーマシューティカルズ インコーポレイテッド Guanylate cyclase agonists and uses thereof
KR102272746B1 (en) 2013-06-05 2021-07-08 보슈 헬스 아일랜드 리미티드 Ultra-pure agonists of guanylate cyclase c, method of making and using same
EP3884935B1 (en) 2013-08-09 2023-06-14 Ardelyx, Inc. Compounds and methods for inhibiting phosphate transport
CA3066872A1 (en) 2017-06-13 2018-12-20 Bayer Aktiengesellschaft Herbicidally active 3-phenylisoxazoline-5-carboxamides of tetrahydro and dihydrofuran carboxamides
SI3638665T1 (en) 2017-06-13 2021-11-30 Bayer Aktiengesellschaft Herbicidal 3-phenylisoxazoline-5-carboxamides of tetrahydro and dihydrofuran carboxylic acids and esters
EP3668845A1 (en) 2017-08-17 2020-06-24 Bayer Aktiengesellschaft Herbicidally active 3-phenyl-5-trifluoromethylisoxazoline-5-carboxamides of cyclopentylcarboxylic acids and esters
JP7217751B2 (en) 2018-01-25 2023-02-03 バイエル・アクチエンゲゼルシヤフト 3-phenylisoxazoline-5-carboxamides of cyclopentenylcarboxylic acid derivatives exhibiting herbicidal activity
ES2950189T3 (en) 2019-03-12 2023-10-05 Bayer Ag 3-Phenylisoxazoline-5-carboxamides of cyclopentenylcarboxylic acid esters containing herbicides
CN114340631A (en) 2019-05-21 2022-04-12 阿德利克斯股份有限公司 Combination for reducing serum phosphate in a patient

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4193926A (en) * 1974-03-20 1980-03-18 Schering Aktiengesellschaft 4-(Polyalkoxy phenyl)-2-pyrrolidones
JPS62103070A (en) * 1985-10-29 1987-05-13 Mitsui Toatsu Chem Inc Isoxazoline derivative and plant growth regulator
US4912120A (en) * 1986-03-14 1990-03-27 Syntex (U.S.A.) Inc. 3,5-substituted 4,5-dihydroisoxazoles as transglutaminase inhibitors
WO1987006576A1 (en) * 1986-04-29 1987-11-05 Pfizer Inc. Calcium independent camp phosphodiesterase inhibitor antidepressant
IE59813B1 (en) * 1986-05-09 1994-04-06 Warner Lambert Co Styryl pyrazoles, isoxazoles and analogs thereof having activity as 5-lipoxy-genase inhibitors and pharmaceutical compositions containing them
ZA872997B (en) * 1986-05-09 1988-12-28 Warner Lambert Co Novel styryl pyrazoles,isoxazoles and analogs thereof having activity as 5-lipoxygenase inhibitors,pharmaceutical compositions and methods of use therefor
DE3736113A1 (en) * 1987-10-26 1989-05-03 Hoechst Ag DRUGS, PHOSPHORUS-BASED 2-ISOXAZOLINES AND ISOXAZOLES CONTAINING THEREOF, AND METHOD OF PREPARING THESE HETEROCYCLIC COMPOUNDS
US4933464A (en) * 1988-04-25 1990-06-12 W. R. Grace & Co.-Conn. Process for forming 3-phenylisoxazolines and 3-phenylisoxazoles
US4952700A (en) * 1988-04-25 1990-08-28 W.R. Grace & Co.-Conn. Preparation of isoxazolines and isoxazoles
CA2017383A1 (en) * 1989-06-08 1990-12-08 Raymond R. Martodam Use of vanilloids for the treatment of respiratory diseases or disorders
WO1991007177A1 (en) * 1989-11-13 1991-05-30 Pfizer Inc. Pyrimidone derivatives and analogs in the treatment of asthma or certain skin disorders
GB9007762D0 (en) * 1990-04-05 1990-06-06 Beecham Group Plc Novel compounds
EP0451790A1 (en) * 1990-04-12 1991-10-16 Hoechst Aktiengesellschaft 3,5-disubstituted 2-isoxazolines and isoxazoles, process for their preparation, medicines containing them and their use
DE4026018A1 (en) * 1990-08-17 1992-02-20 Hoechst Ag PLANT-PROTECTIVE AGENTS CONTAINING ISOXAZOLINE OR ISOTHIAZOLINE AND NEW ISOXAZOLINE AND ISOTHIAZOLINE
AU9030691A (en) * 1990-11-06 1992-05-26 Smithkline Beecham Corporation Imidazolidinone compounds
PT100441A (en) * 1991-05-02 1993-09-30 Smithkline Beecham Corp PIRROLIDINONES, ITS PREPARATION PROCESS, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND USE
AU2869092A (en) * 1991-10-11 1993-05-03 Smithkline Beecham Corporation Heterocyclic 3-phenylpyrrolidin-2-ones, their preparation and use for the manufacture of a medicament for inhibiting tumor necrosis factor production

Also Published As

Publication number Publication date
ATE187447T1 (en) 1999-12-15
DE69422061T2 (en) 2000-03-30
JPH09500146A (en) 1997-01-07
FI945556A0 (en) 1994-11-25
CA2177375A1 (en) 1995-06-01
FI945556A (en) 1995-05-27
GR3032506T3 (en) 2000-05-31
PT730587E (en) 2000-05-31
DE69422061D1 (en) 2000-01-13
WO1995014680A1 (en) 1995-06-01
DK0730587T3 (en) 2000-04-10
US5686434A (en) 1997-11-11
JP2818820B2 (en) 1998-10-30
EP0730587A1 (en) 1996-09-11
EP0730587B1 (en) 1999-12-08

Similar Documents

Publication Publication Date Title
ES2139754T3 (en) 3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS.
BR9408174A (en) Isoxazoline compounds as anti-inflammatory agents
DK0672031T3 (en) Catechol dieters as selective PDE IV inhibitors
FI945555A0 (en) Substituted oxindoles
DK1045690T3 (en) Benzene sulfonamide inhibitors of PDE-IV and their therapeutic use
FR2762841B1 (en) DIAZEPINO-INDOLONES INHIBITING PHOSPHODIESTERASES IV
ATE186528T1 (en) INDOLE-CARBAMATES AS LEUKOTRIENE ANTAGONISTS
DK0752990T3 (en) Benzisothiazole derivatives as inhibitors of 5-lipoxygenase biosynthesis
MX9603943A (en) Isoxazoline compounds as 5-lipoxygenase inhibitors.

Legal Events

Date Code Title Description
FG2A Definitive protection

Ref document number: 730587

Country of ref document: ES